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Acta Obstetricia Et Gynecologica Scandinavica|March 5, 2011
Identification of BRCA1-deficient ovarian cancersAnne-Bine Skytte, Marianne Waldstrøm, Anders Aamann Rasmussen, et al.Human Mutation|October 7, 2006
Genotype-phenotype correlations in von Hippel-Lindau diseaseKai Ren Ong, Emma R Woodward, Pip Killick, et al.International Journal of Cancer|August 22, 2025
Clinical and genetic features of multiple primary tumours cohorts with a renal cell carcinoma: Implications for molecular genetic investigationsHuairen Zhang, Bryndis Yngvadottir, Avgi Andreou, et al.Journal of the National Cancer Institute|August 30, 2008
Germline SDHB mutations and familial renal cell carcinomaChristopher Ricketts, Emma R Woodward, Pip Killick, et al.Familial Cancer|March 13, 2024
Cascade screening in HBOC and Lynch syndrome: guidelines and procedures in a UK centreD Gareth Evans, Kate Green, George J Burghel, et al.Journal of Medical Genetics|January 30, 2021
Targeting lung cancer screening to individuals at greatest risk: the role of genetic factorsMikey B Lebrett, Emma J Crosbie, Miriam J Smith, et al.Journal of Medical Genetics|February 5, 2022
Cost-effectiveness model of renal cell carcinoma (RCC) surveillance in hereditary leiomyomatosis and renal cell carcinoma (HLRCC)Alexander J Thompson, Yousef M Alwan, Vijay A C Ramani, et al.Cancer Biology & Therapy|November 8, 2018
FGFR genes mutation is an independent prognostic factor and associated with lymph node metastasis in squamous non-small cell lung cancerJing Jing Li, Shi Yan, Yaqi Pan, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 28, 2022
High detection rate from genetic testing in BRCA-negative women with familial epithelial ovarian cancerNicola Flaum, Emma J Crosbie, Richard Edmondson, et al.BMJ Oncology|March 6, 2025
UK-based clinical testing programme for somatic and germline BRCA1/2, ATM and CDK12 mutations in prostate cancer: first resultsD Gareth Evans, George Burghel, Helene Schlecht, et al.Pageof 9